PeerJ,
Journal Year:
2024,
Volume and Issue:
12, P. e18413 - e18413
Published: Oct. 31, 2024
Irisin,
a
product
of
the
post-translational
processing
fibronectin
type
III
domain-containing
protein
5
(FNDC5),
is
novel
myokine
which
upregulated
during
exercise.
This
hormone
not
only
promotes
transformation
white
adipose
tissue
into
brown-fat-like
phenotype
but
also
enhances
energy
expenditure
and
mitigates
fat
accumulation.
Its
role
crucial
in
management
certain
metabolic
disorders
such
as
diabetes
heart
disease.
Of
note,
exercise
performed
significantly
affects
blood
irisin
levels,
indicating
critical
physical
activity
regulating
this
hormone.
article
aims
to
summarize
current
scientific
understanding
mechanisms
through
it
mediates
cardiovascular
protection
Moreover,
establish
potential
target
for
preventing
treating
diseases.
PeerJ,
Journal Year:
2024,
Volume and Issue:
12, P. e17267 - e17267
Published: April 29, 2024
Exercise
has
many
beneficial
effects
that
provide
health
and
metabolic
benefits.
Signaling
molecules
are
released
from
organs
tissues
in
response
to
exercise
stimuli
widely
termed
exerkines,
which
exert
influence
on
a
multitude
of
intricate
multi-tissue
processes,
such
as
muscle,
adipose
tissue,
pancreas,
liver,
cardiovascular
kidney,
bone.
For
the
effect,
exerkines
regulate
homeostasis
organisms
by
increasing
glucose
uptake
improving
fat
synthesis.
anti-inflammatory
positively
various
chronic
inflammation-related
diseases,
type
2
diabetes
atherosclerosis.
This
review
highlights
prospective
contribution
regulating
metabolism,
augmenting
effects,
providing
additional
advantages
associated
with
exercise.
Moreover,
comprehensive
overview
analysis
recent
advancements
provided
this
review,
addition
predicting
future
applications
used
potential
biomarker
or
therapeutic
target
benefit
patients
diseases.
Redox Biology,
Journal Year:
2024,
Volume and Issue:
70, P. 103079 - 103079
Published: Feb. 8, 2024
Doxorubicin-induced
cardiotoxicity
(DIC)
adversely
impacts
patients'
long-term
health
and
quality
of
life.
Its
underlying
mechanism
is
complex,
involving
regulatory
cell
death
mechanisms,
such
as
ferroptosis
autophagy.
Moreover,
it
a
challenge
faced
by
patients
undergoing
cardiac
rehabilitation.
Endurance
exercise
(E-Exe)
preconditioning
effectively
counters
DIC
injury,
potentially
through
the
adenosine
monophosphate-activated
protein
kinase
(AMPK)
pathway.
However,
detailed
studies
on
this
process's
mechanisms
are
scarce.
Here,
E-Exe
models
were
established
using
mice
primary
cultured
adult
mouse
cardiomyocytes
(PAMCs).
Akin
to
ferrostatin-1
(ferroptosis
inhibitor),
rapamycin
(autophagic
inducer),
MitoTEMPO
(mitochondrial
free-radical
scavenger),
alleviated
Fe2+
accumulation
oxidative
stress
improved
energy
metabolism
mitochondrial
dysfunction
in
demonstrated
multifunctional,
enzymatic,
morphological
indices.
erastin
3-methyladenine
adenovirus-mediated
AMPKα2
downregulation,
inhibition
compound
C
significantly
diminished
these
effects,
both
vivo
vitro.
The
results
suggest
non-traditional
where
preconditioning,
under
mild
reactive
oxygen
species
generation,
upregulates
phosphorylates
AMPKα2,
thereby
enhancing
complex
I
activity,
activating
adaptive
autophagy,
improving
myocardial
tolerance
injury.
Overall,
study
highlighted
pivotal
role
mitochondria
DIC-induced
shows
how
activated
against
This
suggests
that
could
be
viable
strategy
for
Metabolites,
Journal Year:
2025,
Volume and Issue:
15(1), P. 59 - 59
Published: Jan. 16, 2025
Background/Objectives:
Sarcopenia,
characterized
by
the
progressive
loss
of
muscle
mass
and
strength,
is
linked
to
physical
disability,
metabolic
dysfunction,
an
increased
risk
mortality.
Exercise
therapy
currently
acknowledged
as
a
viable
approach
for
addressing
sarcopenia.
Nevertheless,
molecular
mechanisms
behind
exercise
training
or
activity
remain
poorly
understood.
The
disruption
mitochondrial
homeostasis
implicated
in
pathogenesis
effectively
delays
onset
sarcopenia
significantly
maintaining
homeostasis,
including
promoting
mitophagy,
improving
biogenesis,
balancing
dynamics,
redox.
Exerkines
(e.g.,
adipokines,
myokines,
hepatokines,
osteokines),
signaling
molecules
released
response
training,
may
potentially
contribute
skeletal
metabolism
through
ameliorating
reducing
inflammation,
regulating
protein
synthesis
defense
against
Methods:
In
this
review,
we
provide
detailed
summary
exercise-induced
exerkines
confer
their
benefit,
with
particular
focus
on
impact
context
Results:
induces
substantial
adaptations
muscle,
mass,
improved
regeneration
hypertrophy,
elevated
hormone
release,
enhanced
function.
An
expanding
body
research
highlights
that
have
potential
regulate
processes
such
autophagy,
redox
balance.
These
maintenance
thereby
supporting
health.
Conclusions:
Through
comprehensive
investigation
within
mitochondria,
reveals
new
insights
into
key
exercise-protective
sensors
combating
Journal of Men s Health,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 1, 2024
This
study
was
aimed
to
investigate
the
effects
of
acute
and
chronic
High
Intensity
Interval
Training
(HIIT)
on
Irisin,
BDNF
(brain-derived
neurotrophic
factor),
Apelin
levels.
The
included
twenty-one
male
soccer
referees.
Blood
from
participants
collected
at
beginning
(1.
first
measurement:
baseline
value).
HIIT
conducted
blood
immediately
(2.
second
effect).
Next,
carried
out
for
20
minutes
4
days
a
week
in
bouts
running
(75
meters
seconds)
walking
(25
seconds).
end
12
weeks
(3.
third
performed
again
(4.
fourth
effect
after
There
gradual
increase
irisin,
BDNF,
apelin
levels
(p
<
0.001).
irisin
2%
measurement,
106%
third,
111%
compared
measurement.
39%
116%
133%
fourth.
were
increased
by
11%,
19%and
28%,
respectively.
These
results
demonstrated
that
might
only
response
(4
times
week)
while
change
with
both
healthy
trained
Life Metabolism,
Journal Year:
2024,
Volume and Issue:
3(3)
Published: Feb. 29, 2024
Skeletal
muscle
plays
a
vital
role
in
the
regulation
of
systemic
metabolism,
partly
through
its
secretion
endocrine
factors
which
are
collectively
known
as
myokines.
Altered
myokine
levels
associated
with
metabolic
diseases,
such
type
2
diabetes
(T2D).
The
significance
interorgan
crosstalk,
particularly
myokines,
has
emerged
fundamental
aspect
nutrient
and
energy
homeostasis.
However,
comprehensive
understanding
biology
setting
obesity
T2D
remains
major
challenge.
In
this
review,
we
discuss
biological
functions
key
myokines
that
have
been
extensively
studied
during
past
two
decades,
namely
interleukin
6
(IL-6),
irisin,
myostatin
(MSTN),
growth
differentiation
factor
11
(GDF11),
fibroblast
21
(FGF21),
apelin,
brain-derived
neurotrophic
(BDNF),
meteorin-like
(Metrnl),
secreted
protein
acidic
rich
cysteine
(SPARC),
β-aminoisobutyric
acid
(BAIBA),
Musclin,
Dickkopf
3
(Dkk3).
Related
to
these,
detail
exercise
expression
together
their
contributions
physiology
disease.
Despite
significant
advancements
research,
many
remain
challenging
measure
accurately
investigate
thoroughly.
Hence,
new
research
techniques
detection
methods
should
be
developed
rigorously
tested.
Therefore,
developing
perspective
on
is
crucial,
will
likely
offer
insights
into
pathophysiological
mechanisms
underlying
may
reveal
novel
targets
for
therapeutic
interventions.
Journal of Advanced Research,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 1, 2024
Obesity-induced
bone
loss
affects
the
life
quality
of
patients
all
over
world.
Irisin,
one
myokines,
plays
an
essential
role
in
and
fat
metabolism.
Investigate
effects
irisin
on
metabolism
via
adipocytes
marrow
microenvironment.
In
this
study,
we
fed
fibronectin
type
III
domain-containing
protein
5
(FNDC5,
precursor
irisin)
knockout
mice
(FNDC5-/-)
with
a
high-fat
diet
(HFD)
for
10
weeks.
The
mass
was
assessed
by
micro-CT
analysis,
histological
staining,
dynamic
formation.
vitro,
lipogenic
differentiation
mesenchymal
stem
cells
(BMSCs)
assayed
Oil
Red
O
osteogenic
alkaline
phosphatase
staining.
Meanwhile,
gene
expression
BMSC-differentiated
RNA
sequence
involved
pathway
were
determined
western
blot
qRT-PCR
performed.
FNDC5-/-
HFD
showed
increased
body
weight,
content
bone,
decreased
formation
compared
those
standard
(SD).
inhibited
BMSCs
into
alleviated
inhibition
osteogenesis
derived
from
adipocyte
supernatant.
blocking
experiment
that
reduced
production
interleukin
6
(IL-6)
through
downregulating
TLR4/MyD88/NF-κB
pathway.
Immunofluorescence
staining
further
confirmed
IL-6
SD,
which
suffered
serious
loss.
Irisin
downregulates
activation
pathway,
thereby
reducing
to
enhance
BMSCs.
Thus,
rescue
BMSCs,
initially
IL-6,
is
potential
therapeutic
target
mitigate
obesity-induced
osteoporosis.